Allele Registry

Canonical Allele Identifier: PA286582

Gene: APC HGNC NCBI

ClinVar Allele:

132747

ClinVar RCV:

RCV000115086

RCV000766434

RCV000772714

RCV003764810

RCV003997215

ClinVar Variation:

127290

HGVS (amino-acid)	Matching Registered Transcripts
NP_000029.2:p.Met1211Thr	CA008581 NM_000038.6:c.3632T>C