Allele Registry

Canonical Allele Identifier: PA645482653

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000225026

ClinVar Variation:

236036

HGVS (amino-acid)	Matching Registered Transcripts
NP_004077.1:p.Leu387Phe	CA10581510 NM_004086.3:c.1159C>T