Allele Registry

Canonical Allele Identifier: PA103848

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006994

ClinVar Variation:

6615

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128530.1:p.Cys542Tyr	CA253897 NM_001135058.2:c.1625G>A