Canonical Allele Identifier: PA2827404379
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 1297642
ClinVar RCV Id: RCV001723410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334649.1:p.Gly152Trp
CA389344541
NM_001347720.2:c.454G>T