Allele Registry

Canonical Allele Identifier: PA103937

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006989

ClinVar Variation:

6610

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128530.1:p.Trp117Arg	CA253887 NM_001135058.2:c.349T>C CA389344722 NM_001135058.2:c.349T>A