Allele Registry

Canonical Allele Identifier: PA095621

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000011781

ClinVar Variation:

11034

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Glu63Lys	CA255653 NM_001399.5:c.187G>A