Allele Registry

Canonical Allele Identifier: PA2828003728

Gene: APC HGNC NCBI

ClinVar Allele:

180220

ClinVar RCV:

RCV000204441

RCV000216441

RCV000656749

RCV003650407

RCV003998419

ClinVar Variation:

181815

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341831.1:p.His2141Asp	CA012407 NM_001354902.2:c.6421C>G