Allele Registry

Canonical Allele Identifier: PA253892

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006991

RCV001532242

ClinVar Variation:

6612

HGVS (amino-acid)	Matching Registered Transcripts
NP_004077.1:p.Ile109Asn	CA253891 NM_004086.3:c.326T>A