Canonical Allele Identifier: PA166808
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_000029.2:p.Arg216Gly
CA012188
NM_000038.6:c.646C>G