Allele Registry

Canonical Allele Identifier: PA916041565

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000572011

RCV003742797

ClinVar Variation:

470108

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341825.1:p.His2609Pro	CA049129 NM_001354896.2:c.7826A>C