Allele Registry

Canonical Allele Identifier: PA095444

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000011783

RCV000414306

RCV003390668

ClinVar Variation:

11036

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Arg156Cys	CA255655 NM_001399.5:c.466C>T