Allele Registry

Canonical Allele Identifier: PA156887

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000120048

RCV000122774

RCV000568279

RCV001704031

RCV003650380

RCV003905137

RCV003997337

ClinVar Variation:

133538

HGVS (amino-acid)	Matching Registered Transcripts
NP_000029.2:p.Met1211Arg	CA008588 NM_000038.6:c.3632T>G