Canonical Allele Identifier: PA1139720185
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 947067

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Ala9Asp
CA5667578
NM_016169.4:c.26C>A