Canonical Allele Identifier: PA2827404384
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_001334649.1:p.Arg156Gly
CA258536569
NM_001347720.2:c.466C>G