Canonical Allele Identifier: PA2825274443
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 1169716
ClinVar RCV Id: RCV001521383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Thr275Ser
CA10439015
NM_001005612.3:c.824C>G
CA413448837
NM_001005612.3:c.823A>T