Allele Registry

Canonical Allele Identifier: PA095853

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000155912

ClinVar Variation:

179127

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Lys158Asn	CA273588 NM_001399.5:c.474A>C CA413447981 NM_001399.5:c.474A>T