Allele Registry

Canonical Allele Identifier: PA095944

Gene: EDA HGNC NCBI

ClinVar Allele:

26087

ClinVar RCV:

RCV000011795

RCV001205829

ClinVar Variation:

11048

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Thr338Met	CA121314 NM_001399.5:c.1013C>T