Canonical Allele Identifier: PA915990487
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 642318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Ala22Val
CA212238105
NM_016169.4:c.65C>T