Allele Registry

Canonical Allele Identifier: PA658660356

Gene: APC HGNC NCBI

ClinVar RCV:

RCV002358548

RCV003470762

ClinVar Variation:

470050

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Pro2170Ser	CA16035571 NM_001127510.3:c.6508C>T