Canonical Allele Identifier: PA645431301
Gene: SF3B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006833.2:p.Glu700Gly
CA16602960
NM_006842.3:c.2099A>G