Allele Registry

Canonical Allele Identifier: PA095611

Gene: EDA HGNC NCBI

ClinVar Allele:

26084

ClinVar RCV:

RCV000011792

ClinVar Variation:

11045

HGVS (amino-acid)	Matching Registered Transcripts
NP_001390.1:p.Gln358Glu	CA121313 NM_001399.5:c.1072C>G