Canonical Allele Identifier: PA156868
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg2530Gln
CA013904
NM_001127510.3:c.7589G>A