Canonical Allele Identifier: PA2826140669
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 406384
ClinVar RCV Id: RCV000474319 RCV002365622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Ala22Gly
CA5667586
NM_001178133.2:c.65C>G