Canonical Allele Identifier: PA2826140602
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 666154
ClinVar RCV Id: RCV000824588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Ala2Val
CA377886005
NM_001178133.2:c.5C>T