Allele Registry

Canonical Allele Identifier: PA261492

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000037172

ClinVar Variation:

44194

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Arg156Leu	CA261491 NM_001399.5:c.467G>T