Canonical Allele Identifier: PA2741910076
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 2644150
ClinVar RCV Id: RCV003425008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004077.1:p.Arg91Gly
CA258536569
NM_004086.3:c.271C>G