Canonical Allele Identifier: PA2573079652
Gene: SBF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 645714
ClinVar RCV Id: RCV000799856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373268.1:p.Ser1766Arg
CA379631495
NM_001386339.1:c.5298C>G
CA379631496
NM_001386339.1:c.5298C>A
CA379631502
NM_001386339.1:c.5296A>C