Allele Registry

Canonical Allele Identifier: PA916041278

Gene: APC HGNC NCBI

ClinVar Allele:

406586

ClinVar RCV:

RCV000479194

RCV002367649

RCV003766710

ClinVar Variation:

422747

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341825.1:p.Ser2361Phe	CA16036653 NM_001354896.2:c.7082C>T