symbol withdrawn CMH2

Preferred Label : symbol withdrawn CMH2;

Obsolete resource : true;

Approved symbol HGNC : CMH2;

Chromosome HGNC : 1q32;

Locus type HGNC : phenotype;

Détails

Origin ID

HGNC:2114;

Automatic exact mappings (from CISMeF team)
- Cardiomyopathy, familial hypertrophic, 2 [OMIM Phenotype]
Replaced by
- troponin T2, cardiac type [HGNC gene]

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