Allele Registry

Canonical Allele Identifier: PA2825788352

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000155766

ClinVar Variation:

178988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128530.1:p.Gly88Val	CA183442 NM_001135058.2:c.263G>T