Canonical Allele Identifier: PA143928
Gene: SBF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 51005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002963.2:p.Met417Val
CA143927
NM_002972.4:c.1249A>G