Canonical Allele Identifier: PA174555
Gene: SF3B3 HGNC NCBI

Linked Data

ClinVar Variation Id: 161663
ClinVar RCV Id: RCV000149199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036558.3:p.Gly501Trp
CA174554
NM_012426.5:c.1501G>T