Canonical Allele Identifier: PA2826140821
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 406392
ClinVar RCV Id: RCV000476504 RCV000763640 RCV001293037 RCV001016523 RCV003105911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Ser92Thr
CA5667641
NM_001178133.2:c.275G>C