Canonical Allele Identifier: PA2826140676
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 1016982
ClinVar RCV Id: RCV001316062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Pro23Ala
CA377886330
NM_001178133.2:c.67C>G