Canonical Allele Identifier: PA915990452
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 666154
ClinVar RCV Id: RCV000824588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Ala2Val
CA377886005
NM_016169.4:c.5C>T