Canonical Allele Identifier: PA2573268988
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 1522672
ClinVar Variation Id: 1735036
ClinVar RCV Id: RCV002363950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Thr13Ser
CA5667580
NM_016169.4:c.38C>G
CA377886204
NM_016169.4:c.37A>T