Canonical Allele Identifier: PA2828006580
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro1382Arg
CA16031465
NM_001354905.2:c.4145C>G