Canonical Allele Identifier: PA2829111111
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 306606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Glu464Lys
CA5881810
NM_001386342.1:c.1390G>A