Canonical Allele Identifier: PA916042002
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233215
ClinVar Variation Id: 862543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser987Arg
CA10578350
NM_001354900.2:c.2961T>A
CA16028081
NM_001354900.2:c.2959A>C
CA16028087
NM_001354900.2:c.2961T>G