Canonical Allele Identifier: PA2826140632
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 2921792
ClinVar RCV Id: RCV003782814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Pro12Ser
CA377886176
NM_001178133.2:c.34C>T