Canonical Allele Identifier: PA261485
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44190
ClinVar RCV Id: RCV000037166 RCV000255907 RCV001814027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Met1Thr