Canonical Allele Identifier: PA2828004210
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2826000
ClinVar RCV Id: RCV003744245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His2463Leu
CA16037977
NM_001354902.2:c.7388A>T