Allele Registry

Canonical Allele Identifier: PA103884

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006991

RCV001532242

ClinVar Variation:

6612

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128530.1:p.Ile109Asn	CA253891 NM_001135058.2:c.326T>A