Canonical Allele Identifier: PA2829110727
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246568
ClinVar RCV Id: RCV000235333 RCV000303226 RCV001094187 RCV002365232 RCV001820788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373268.1:p.Ser1252Cys
CA5881173
NM_001386339.1:c.3754A>T