Canonical Allele Identifier: PA2573079666
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 861873
ClinVar RCV Id: RCV001068485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373268.1:p.Ala1832Val
CA5880714
NM_001386339.1:c.5495C>T