Canonical Allele Identifier: PA184076
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 179264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Asp265Gly
CA184075
NM_001399.5:c.794A>G