Allele Registry

Canonical Allele Identifier: PA297763

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000159537

RCV000491278

RCV000766428

RCV001353861

RCV003534402

RCV003998407

ClinVar Variation:

181791

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120983.2:p.Gly617Ala	CA006287 NM_001127511.3:c.1850G>C