Canonical Allele Identifier: PA2826140613
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 1380808
ClinVar RCV Id: RCV001917319 RCV002425170
ClinVar Variation Id: 2009618
ClinVar RCV Id: RCV002842542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Ser7Arg
CA377886110
NM_001178133.2:c.19A>C
CA377886118
NM_001178133.2:c.21C>A
CA377886119
NM_001178133.2:c.21C>G