Canonical Allele Identifier: PA645401969
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411553
ClinVar RCV Id: RCV003766600
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg2305Gly
CA16036410
NM_001127510.3:c.6913A>G