Allele Registry

Canonical Allele Identifier: PA658676732

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000521166

RCV001212052

ClinVar Variation:

451339

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Pro216Ser	CA413448418 NM_001399.5:c.646C>T