Canonical Allele Identifier: PA645484294
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 418174
ClinVar RCV Id: RCV000480786 RCV001851133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Ala382Thr
CA16621477
NM_001399.5:c.1144G>A