Canonical Allele Identifier: PA2828048049
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro2396Arg
CA16037774
NM_001354904.2:c.7187C>G