Canonical Allele Identifier: PA2829111485
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 225113
ClinVar RCV Id: RCV000210731 RCV001853377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.His1158Arg
CA358258
NM_001386342.1:c.3473A>G