Canonical Allele Identifier: PA2829111551
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 225095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Val1243Ala
CA358114
NM_001386342.1:c.3728T>C