Allele Registry

Canonical Allele Identifier: PA156786

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000120027

RCV003764835

ClinVar Variation:

133520

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120983.2:p.Pro2234Ala	CA012481 NM_001127511.3:c.6700C>G