Canonical Allele Identifier: PA2826140629
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 3226880
ClinVar RCV Id: RCV004522046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Pro12Arg
CA377886184
NM_001178133.2:c.35C>G