Allele Registry

Canonical Allele Identifier: PA658660805

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000572011

RCV003742797

ClinVar Variation:

470108

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.His2591Pro	CA049129 NM_001127510.3:c.7772A>C