Canonical Allele Identifier: PA2828008701
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Arg1760Gly
CA010637
NM_001354905.2:c.5278C>G