Allele Registry

Canonical Allele Identifier: PA095900

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000011785

RCV000154610

ClinVar Variation:

11038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Pro209Leu	CA181048 NM_001399.5:c.626C>T