Allele Registry

Canonical Allele Identifier: PA645399104

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000213818

RCV001200168

RCV001800574

RCV002515704

RCV002554571

RCV003650592

RCV003743671

ClinVar Variation:

233215

862543

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Ser1028Arg	CA10578350 NM_001127510.3:c.3084T>A CA16028081 NM_001127510.3:c.3082A>C CA16028087 NM_001127510.3:c.3084T>G