Canonical Allele Identifier: PA2828188309
Gene: SBF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503306
ClinVar RCV Id: RCV002045399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352748.1:p.Gly1543Arg
CA412193615
NM_001365819.1:c.4627G>C
CA412193617
NM_001365819.1:c.4627G>A