Allele Registry

Canonical Allele Identifier: PA645484210

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000489664

RCV003479140

ClinVar Variation:

426389

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Tyr311His	CA413449247 NM_001399.5:c.931T>C