Allele Registry

Canonical Allele Identifier: PA297892

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000159568

RCV000219951

RCV000409928

RCV001192797

RCV003315949

RCV003998420

ClinVar Variation:

181816

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Pro2392Thr	CA012891 NM_001127510.3:c.7174C>A