Canonical Allele Identifier: PA169271
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142731
ClinVar RCV Id: RCV000132104 RCV000590671 RCV002514750 RCV002265621 RCV003998132
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg1450Gln
CA009471
NM_001127510.3:c.4349G>A