Canonical Allele Identifier: PA2825788351
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_001128530.1:p.Gly87Ala
CA389344544
NM_001135058.2:c.260G>C