Canonical Allele Identifier: PA658676732
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 451339
ClinVar RCV Id: RCV000521166 RCV001212052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Pro216Ser
CA413448418
NM_001399.5:c.646C>T