Allele Registry

Canonical Allele Identifier: PA916029223

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006994

ClinVar Variation:

6615

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334649.1:p.Cys607Tyr	CA253897 NM_001347720.2:c.1820G>A