Canonical Allele Identifier: PA2825274619
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11031
ClinVar RCV Id: RCV000011778 RCV000763629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005613.1:p.Tyr61His
CA255649
NM_001005613.4:c.181T>C