Canonical Allele Identifier: PA2829111820
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 861873
ClinVar RCV Id: RCV001068485
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Ala1757Val
CA5880714
NM_001386342.1:c.5270C>T