Canonical Allele Identifier: PA358260
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 225113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112224.1:p.His1201Arg
CA358258
NM_030962.4:c.3602A>G