Allele Registry

Canonical Allele Identifier: PA2828001378

Gene: APC HGNC NCBI

ClinVar Variation Id: 1315725

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341831.1:p.Asp925Tyr	CA16028002 NM_001354902.2:c.2773G>T