Canonical Allele Identifier: PA658814397
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 524666
ClinVar RCV Id: RCV000628510 RCV001016349 RCV003459485 RCV003237957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Ala9Val
CA377886134
NM_016169.4:c.26C>T