Allele Registry

Canonical Allele Identifier: PA175987

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000150604

ClinVar Variation:

163322

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Gln306Leu	CA175986 NM_001399.5:c.917A>T