Canonical Allele Identifier: PA358116
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 225095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112224.1:p.Val1286Ala
CA358114
NM_030962.4:c.3857T>C