Canonical Allele Identifier: PA645484165
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 228257
ClinVar RCV Id: RCV000223248 RCV001054886 RCV001248822 RCV003317157 RCV003886387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Arg289His
CA10577177
NM_001399.5:c.866G>A