Canonical Allele Identifier: PA645484269
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 265112
ClinVar RCV Id: RCV000255432 RCV000532383 RCV002287400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Arg357Trp
CA10588798
NM_001399.5:c.1069C>T