Allele Registry

Canonical Allele Identifier: PA2827947916

Gene: APC HGNC NCBI

ClinVar Variation Id: 490365

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341824.1:p.Phe2620Leu	CA16038407 NM_001354895.2:c.7858T>C CA16038412 NM_001354895.2:c.7860T>A CA16038413 NM_001354895.2:c.7860T>G