Allele Registry

Canonical Allele Identifier: PA103832

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006992

RCV000710321

ClinVar Variation:

6613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128530.1:p.Ala119Thr	CA253893 NM_001135058.2:c.355G>A