Canonical Allele Identifier: PA095422
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44193
ClinVar RCV Id: RCV000420111 RCV000592238 RCV003478983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Arg153Cys
CA261490
NM_001399.5:c.457C>T