Canonical Allele Identifier: PA2829111793
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 645714
ClinVar RCV Id: RCV000799856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Ser1691Arg
CA379631495
NM_001386342.1:c.5073C>G
CA379631496
NM_001386342.1:c.5073C>A
CA379631502
NM_001386342.1:c.5071A>C