Canonical Allele Identifier: PA095439
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11035
ClinVar RCV Id: RCV000011782 RCV000254983 RCV000763630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Arg155Cys
CA255654
NM_001399.5:c.463C>T