Canonical Allele Identifier: PA156886
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133538
ClinVar RCV Id: RCV000120048 RCV000122774 RCV000568279 RCV003650380 RCV003997337 RCV003905137 RCV001704031
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Met1193Arg
CA008588
NM_001127511.3:c.3578T>G