Allele Registry

Canonical Allele Identifier: PA2827975649

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000213818

RCV001200168

RCV001800574

RCV002515704

RCV002554571

RCV003650592

RCV003743671

ClinVar Variation:

233215

862543

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341828.1:p.Ser1000Arg	CA10578350 NM_001354899.2:c.3000T>A CA16028081 NM_001354899.2:c.2998A>C CA16028087 NM_001354899.2:c.3000T>G