Canonical Allele Identifier: PA2825273968
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 1457978
ClinVar RCV Id: RCV001949391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Gly207Arg
CA413448360
NM_001005609.2:c.619G>A
CA413448361
NM_001005609.2:c.619G>C