Canonical Allele Identifier: PA156888
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133538
ClinVar RCV Id: RCV000120048 RCV000122774 RCV000568279 RCV003650380 RCV003997337 RCV003905137 RCV001704031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met1211Arg
CA008588
NM_001127510.3:c.3632T>G