Canonical Allele Identifier: PA645482165
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 406384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Ala22Gly
CA5667586
NM_016169.4:c.65C>G