Canonical Allele Identifier: PA2826140638
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_001171604.1:p.Thr13Ser
CA5667580
NM_001178133.2:c.38C>G
CA377886204
NM_001178133.2:c.37A>T