Canonical Allele Identifier: PA2825788438
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 1305492
ClinVar RCV Id: RCV001768699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128530.1:p.Arg416His
CA258541191
NM_001135058.2:c.1247G>A