Canonical Allele Identifier: PA2573079681
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Gln976Leu
CA5881388
NM_001386342.1:c.2927A>T