Allele Registry

Canonical Allele Identifier: PA916029219

Gene: COCH HGNC NCBI

ClinVar RCV:

RCV000006995

ClinVar Variation:

6616

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334649.1:p.Met577Thr	CA253899 NM_001347720.2:c.1730T>C