Canonical Allele Identifier: PA658676725
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 458656
ClinVar RCV Id: RCV000544580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Arg159Thr
CA413447985
NM_001399.5:c.476G>C