Canonical Allele Identifier: PA2825274058
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Gly299Ser
CA261509
NM_001005609.2:c.895G>A