Canonical Allele Identifier: PA2499257701
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 1169716
ClinVar RCV Id: RCV001521383
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Thr278Ser
CA10439015
NM_001399.5:c.833C>G
CA413448837
NM_001399.5:c.832A>T