Canonical Allele Identifier: PA2829110375
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_001373268.1:p.Cys656Ser
CA5881669
NM_001386339.1:c.1967G>C
CA379642352
NM_001386339.1:c.1966T>A