Canonical Allele Identifier: PA2826140647
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 2055680
ClinVar RCV Id: RCV002938160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Pro16Ala
CA377886246
NM_001178133.2:c.46C>G