Canonical Allele Identifier: PA1139746691
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_112224.1:p.Ala1800Val
CA5880714
NM_030962.4:c.5399C>T