Canonical Allele Identifier: PA2828004208
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2065558
ClinVar RCV Id: RCV003744826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His2463Arg
CA16037976
NM_001354902.2:c.7388A>G