Canonical Allele Identifier: PA166809
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141927
ClinVar RCV Id: RCV000130641 RCV003764868
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg216Gly
CA012188
NM_001127510.3:c.646C>G