Canonical Allele Identifier: PA2825274475
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 228258
ClinVar RCV Id: RCV000214953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Tyr301Ser
CA10577178
NM_001005612.3:c.902A>C