Canonical Allele Identifier: PA095762
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 253056
ClinVar RCV Id: RCV000239466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.His252Leu
CA10586174
NM_001399.5:c.755A>T