Allele Registry

Canonical Allele Identifier: PA2828000646

Gene: APC HGNC NCBI

ClinVar RCV:

RCV001188921

RCV002560936

ClinVar Variation:

926362

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341831.1:p.Leu538Ser	CA16025442 NM_001354902.2:c.1613T>C