Canonical Allele Identifier: PA2826141318
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 406398
ClinVar RCV Id: RCV000464552 RCV001017160 RCV002480368 RCV003463873 RCV003333747 RCV003483616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Thr353Met
CA5667865
NM_001178133.2:c.1058C>T