Allele Registry

Canonical Allele Identifier: PA2828042449

Gene: APC HGNC NCBI

ClinVar RCV:

RCV001189874

RCV001775866

RCV003742727

ClinVar Variation:

469991

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341833.1:p.Thr1583Ser	CA16032532 NM_001354904.2:c.4747A>T CA16032534 NM_001354904.2:c.4748C>G