Canonical Allele Identifier: PA645484035
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 228256
ClinVar RCV Id: RCV000218495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Arg159Ser
CA10577172
NM_001399.5:c.477A>T
CA413447987
NM_001399.5:c.477A>C