Canonical Allele Identifier: PA2829110298
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 306606
ClinVar RCV Id: RCV000654076 RCV001172806 RCV001094221 RCV002392844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373268.1:p.Glu507Lys
CA5881810
NM_001386339.1:c.1519G>A