Allele Registry

Canonical Allele Identifier: PA2828016569

Gene: APC HGNC NCBI

ClinVar RCV:

RCV001188921

RCV002560936

ClinVar Variation:

926362

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341832.1:p.Leu528Ser	CA16025442 NM_001354903.2:c.1583T>C