Allele Registry

Canonical Allele Identifier: PA916029202

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006989

ClinVar Variation:

6610

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334649.1:p.Trp182Arg	CA253887 NM_001347720.2:c.544T>C CA389344722 NM_001347720.2:c.544T>A