Allele Registry

Canonical Allele Identifier: PA916041597

Gene: APC HGNC NCBI

ClinVar Variation Id: 490365

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341825.1:p.Phe2638Leu	CA16038407 NM_001354896.2:c.7912T>C CA16038412 NM_001354896.2:c.7914T>A CA16038413 NM_001354896.2:c.7914T>G