Canonical Allele Identifier: PA2829111258
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 194989
ClinVar RCV Id: RCV000175483 RCV000438792 RCV000206768 RCV001094125 RCV001173128 RCV001293356 RCV003937583 RCV002444702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Gly732Ser
CA201480
NM_001386342.1:c.2194G>A