Canonical Allele Identifier: PA162218
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 135283
ClinVar RCV Id: RCV000122098 RCV000471241 RCV000562404 RCV000763642 RCV000726658 RCV003460861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Ser349Gly
CA162216
NM_016169.4:c.1045A>G