symbol withdrawn HSCR2

Preferred Label : symbol withdrawn HSCR2;

Obsolete resource : true;

Approved symbol HGNC : HSCR2;

Chromosome HGNC : 13q21-q32.1 or 13q32.3-q33.2;

Locus type HGNC : other;

Details

Origin ID

HGNC:5207;

Automatic exact mappings (from CISMeF team)
- Hirschsprung disease, susceptibility to, 2 [OMIM Phenotype]
Replaced by
- endothelin receptor type B [HGNC gene]

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