Canonical Allele Identifier: PA2826140674
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 1010561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Ala22Asp
CA377886325
NM_001178133.2:c.65C>A