Canonical Allele Identifier: PA916040471
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro1684Arg
CA040334
NM_001354896.2:c.5051C>G