Allele Registry

Canonical Allele Identifier: PA095677

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000011786

ClinVar Variation:

11039

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Gly224Ala	CA255656 NM_001399.5:c.671G>C