Canonical Allele Identifier: PA2826140608
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 956096
ClinVar RCV Id: RCV001228839 RCV002393565 RCV003462780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Arg5Trp
CA212238071
NM_001178133.2:c.13C>T