Allele Registry

Canonical Allele Identifier: PA253884

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006987

ClinVar Variation:

6608

HGVS (amino-acid)	Matching Registered Transcripts
NP_004077.1:p.Val66Gly	CA253883 NM_004086.3:c.197T>G