Canonical Allele Identifier: PA2828022836
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg1357Gln
CA009812
NM_001354906.2:c.4070G>A