Canonical Allele Identifier: PA658655081
Gene: SUFU HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.His176Arg
CA377908386
NM_016169.4:c.527A>G