Canonical Allele Identifier: PA095900
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11038
ClinVar RCV Id: RCV000011785 RCV000154610
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Pro209Leu
CA181048
NM_001399.5:c.626C>T