Canonical Allele Identifier: PA2825274468
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44213
ClinVar RCV Id: RCV000037191 RCV001778676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Gly296Ser
CA261509
NM_001005612.3:c.886G>A