Canonical Allele Identifier: PA658808059
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 528356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Phe314Ser
CA413449333
NM_001399.5:c.941T>C