Canonical Allele Identifier: PA133748
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44195
ClinVar RCV Id: RCV000037173 RCV000990855
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Glu164Ala
CA133747
NM_001399.5:c.491A>C