Canonical Allele Identifier: PA2825788436
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 313004
ClinVar RCV Id: RCV000340373 RCV000506683 RCV000755239 RCV003950064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128530.1:p.Ile402Val
CA7143286
NM_001135058.2:c.1204A>G