Canonical Allele Identifier: PA2825274342
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Arg155Cys
CA255654
NM_001005612.3:c.463C>T