Allele Registry

Canonical Allele Identifier: PA2827404382

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006988

RCV003555950

ClinVar Variation:

6609

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334649.1:p.Gly153Glu	CA253885 NM_001347720.2:c.458G>A