Canonical Allele Identifier: PA095444
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11036
ClinVar RCV Id: RCV000011783 RCV000414306 RCV003390668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Arg156Cys
CA255655
NM_001399.5:c.466C>T