Canonical Allele Identifier: PA2826140611
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 1054599
ClinVar RCV Id: RCV001363131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Pro6Arg
CA377886100
NM_001178133.2:c.17C>G