Canonical Allele Identifier: PA2825788354
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 2644150
ClinVar RCV Id: RCV003425008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128530.1:p.Arg91Gly
CA258536569
NM_001135058.2:c.271C>G