Canonical Allele Identifier: PA143930
Gene: SBF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 51006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002963.2:p.Thr1590Ala
CA143929
NM_002972.4:c.4768A>G