Allele Registry

Canonical Allele Identifier: PA103945

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006987

ClinVar Variation:

6608

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128530.1:p.Val66Gly	CA253883 NM_001135058.2:c.197T>G