Canonical Allele Identifier: PA286642
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127308
ClinVar RCV Id: RCV000115106 RCV000562980 RCV003153365 RCV003997224 RCV002228239 RCV003474709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg1920Gly
CA010637
NM_000038.6:c.5758C>G