Canonical Allele Identifier: PA116363
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 3569
ClinVar RCV Id: RCV000003750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Pro15Leu
CA116361
NM_016169.4:c.44C>T