Allele Registry

Canonical Allele Identifier: PA261502

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000037181

ClinVar Variation:

44203

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Pro203Ser	CA261501 NM_001399.5:c.607C>T