Canonical Allele Identifier: PA2829111189
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 429748
ClinVar RCV Id: RCV000493165 RCV000763789 RCV000526990 RCV000766678 RCV002420258 RCV001173111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Cys613Ser
CA5881669
NM_001386342.1:c.1838G>C
CA379642352
NM_001386342.1:c.1837T>A