Canonical Allele Identifier: PA095935
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 1070895
ClinVar RCV Id: RCV001383224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Thr211Arg
CA413448388
NM_001399.5:c.632C>G