Canonical Allele Identifier: PA916040604
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys1789Arg
CA16032947
NM_001354896.2:c.5366A>G