Canonical Allele Identifier: PA2829111840
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 306574
ClinVar RCV Id: RCV000268409
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Ala1792Thr
CA10631790
NM_001386342.1:c.5374G>A