Allele Registry

Canonical Allele Identifier: PA2825274619

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000011778

RCV000763629

ClinVar Variation:

11031

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005613.1:p.Tyr61His	CA255649 NM_001005613.4:c.181T>C