symbol withdrawn WS2A

Preferred Label : symbol withdrawn WS2A;

Obsolete resource : true;

Approved symbol HGNC : WS2A;

Chromosome HGNC : 3p14.2-p13;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:12793;

Automatic exact mappings (from CISMeF team)
- Waardenburg syndrome, type 2a [OMIM Phenotype]
Replaced by
- melanocyte inducing transcription factor [HGNC gene]

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