Canonical Allele Identifier: PA2829111764
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220725
ClinVar RCV Id: RCV000206356 RCV000268529 RCV001173798 RCV001000985 RCV002227459 RCV003967553 RCV002336565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373271.1:p.Arg1643Ser
CA350400
NM_001386342.1:c.4929A>T
CA379631795
NM_001386342.1:c.4929A>C