Canonical Allele Identifier: PA261502
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44203
ClinVar RCV Id: RCV000037181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Pro203Ser
CA261501
NM_001399.5:c.607C>T