Canonical Allele Identifier: PA2826140641
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 453965

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Pro15Thr
CA5667582
NM_001178133.2:c.43C>A