Allele Registry

Canonical Allele Identifier: PA2827404374

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006987

ClinVar Variation:

6608

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334649.1:p.Val131Gly	CA253883 NM_001347720.2:c.392T>G