Canonical Allele Identifier: PA2826140945
Gene: SUFU HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.His176Arg
CA377908386
NM_001178133.2:c.527A>G