Canonical Allele Identifier: PA1139746621
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 840713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112224.1:p.Ser1692Pro
CA5880790
NM_030962.4:c.5074T>C