Canonical Allele Identifier: PA2829111826
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039338
ClinVar RCV Id: RCV001342793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Asp1769Gly
CA379630025
NM_001386342.1:c.5306A>G