Allele Registry

Canonical Allele Identifier: PA103911

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006995

ClinVar Variation:

6616

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128530.1:p.Met512Thr	CA253899 NM_001135058.2:c.1535T>C