Canonical Allele Identifier: PA2826140677
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 2929189
ClinVar RCV Id: RCV003781915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Pro23Arg
CA377886336
NM_001178133.2:c.68C>G