Canonical Allele Identifier: PA2825023727
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411553
ClinVar RCV Id: RCV003766600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg2305Gly
CA16036410
NM_000038.6:c.6913A>G