Allele Registry

Canonical Allele Identifier: PA916040222

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000122780

RCV000567758

RCV001284708

ClinVar Variation:

135702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341825.1:p.Thr1463Ala	CA009444 NM_001354896.2:c.4387A>G