Canonical Allele Identifier: PA2826140628
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 1733067
ClinVar RCV Id: RCV002346596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Pro12His
CA377886189
NM_001178133.2:c.35C>A