Allele Registry

Canonical Allele Identifier: PA103878

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006988

RCV003555950

ClinVar Variation:

6609

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128530.1:p.Gly88Glu	CA253885 NM_001135058.2:c.263G>A