Canonical Allele Identifier: PA1139720170
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 956096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Arg5Trp
CA212238071
NM_016169.4:c.13C>T