Canonical Allele Identifier: PA095853
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 179127
ClinVar RCV Id: RCV000155912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Lys158Asn
CA273588
NM_001399.5:c.474A>C
CA413447981
NM_001399.5:c.474A>T