Allele Registry

Canonical Allele Identifier: PA2827404381

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000155766

ClinVar Variation:

178988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334649.1:p.Gly153Val	CA183442 NM_001347720.2:c.458G>T