Canonical Allele Identifier: PA103911
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 6616
ClinVar RCV Id: RCV000006995

Amino-acid Alleles

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