Canonical Allele Identifier: PA2830067290
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039338
ClinVar RCV Id: RCV001342793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112224.1:p.Asp1812Gly
CA379630025
NM_030962.4:c.5435A>G