Allele Registry

Canonical Allele Identifier: PA2827965001

Gene: APC HGNC NCBI

ClinVar RCV:

RCV003536633

ClinVar Variation:

2748653

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341827.1:p.Ser521Gly	CA16024881 NM_001354898.2:c.1561A>G CA2697546184 NM_001354898.2:c.1560_1561delinsAG