Canonical Allele Identifier: PA2580399457
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 2055680
ClinVar RCV Id: RCV002938160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Pro16Ala
CA377886246
NM_016169.4:c.46C>G