Canonical Allele Identifier: PA891851690
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 568531
ClinVar RCV Id: RCV000688921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Gly8Cys
CA377886123
NM_016169.4:c.22G>T