Canonical Allele Identifier: PA915990477
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 802631
ClinVar RCV Id: RCV000988446 RCV003238258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Thr13Pro
CA377886198
NM_016169.4:c.37A>C