Canonical Allele Identifier: PA2825274032
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 1169716
ClinVar RCV Id: RCV001521383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Thr278Ser
CA10439015
NM_001005609.2:c.833C>G
CA413448837
NM_001005609.2:c.832A>T