Allele Registry

Canonical Allele Identifier: PA916029201

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006991

RCV001532242

ClinVar Variation:

6612

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334649.1:p.Ile174Asn	CA253891 NM_001347720.2:c.521T>A