Canonical Allele Identifier: PA095677
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11039
ClinVar RCV Id: RCV000011786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Gly224Ala
CA255656
NM_001399.5:c.671G>C