Allele Registry

Canonical Allele Identifier: PA297861

Gene: APC HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000122787

RCV000159562

RCV000210078

RCV000210900

RCV000211923

RCV000656747

RCV000764567

RCV001155575

RCV003398739

RCV003534359

ClinVar Variation:

135709

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000029.2:p.Pro1934Leu	CA010706 NM_000038.6:c.5801C>T