Canonical Allele Identifier: PA2825274520
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11048
ClinVar RCV Id: RCV000011795 RCV001205829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Thr333Met
CA121314
NM_001005612.3:c.998C>T