Canonical Allele Identifier: PA2828005667
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Glu1157Gln
CA008815
NM_001354905.2:c.3469G>C