Canonical Allele Identifier: PA2827952937
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2567068
ClinVar RCV Id: RCV003311060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly2311Ala
CA16036342
NM_001354896.2:c.6932G>C