Canonical Allele Identifier: PA261506
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44209
ClinVar RCV Id: RCV000037187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Trp274Cys
CA261505
NM_001399.5:c.822G>T
CA413448817
NM_001399.5:c.822G>C