Canonical Allele Identifier: PA2826140651
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 1744670
ClinVar RCV Id: RCV002343020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Ala17Pro
CA377886254
NM_001178133.2:c.49G>C