Canonical Allele Identifier: PA645472939
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 306600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112224.1:p.Gln733Glu
CA5881611
NM_030962.4:c.2197C>G