Canonical Allele Identifier: PA2825274351
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 458656
ClinVar RCV Id: RCV000544580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Arg159Thr
CA413447985
NM_001005612.3:c.476G>C