Allele Registry

Canonical Allele Identifier: PA156783

Gene: APC HGNC NCBI

ClinVar Allele:

137258

ClinVar RCV:

RCV000120026

RCV000129039

RCV000198586

RCV000657042

RCV003534350

ClinVar Variation:

133519

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Thr1292Met	CA008722 NM_001127510.3:c.3875C>T