Canonical Allele Identifier: PA2827404380
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 517362
ClinVar RCV Id: RCV000605898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334649.1:p.Gly152Ala
CA389344544
NM_001347720.2:c.455G>C