Canonical Allele Identifier: PA260053
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 31908
ClinVar RCV Id: RCV000024599 RCV000626808 RCV002262574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Arg276Cys
CA260052
NM_001399.5:c.826C>T