Canonical Allele Identifier: PA2828013397
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro2509Arg
CA16038725
NM_001354905.2:c.7526C>G