Allele Registry

Canonical Allele Identifier: PA658660434

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000569441

RCV003537179

ClinVar Variation:

485093

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Pro2284Leu	CA16036289 NM_001127510.3:c.6851C>T