Canonical Allele Identifier: PA658655081
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 446157
ClinVar RCV Id: RCV000515250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.His176Arg
CA377908386
NM_016169.4:c.527A>G