Allele Registry

Canonical Allele Identifier: PA916029211

Gene: COCH HGNC NCBI

ClinVar Allele:

802077

ClinVar RCV:

RCV001004791

RCV003558639

ClinVar Variation:

813819

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334649.1:p.Ile437Thr	CA389348313 NM_001347720.2:c.1310T>C