Canonical Allele Identifier: PA2827953290
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2065558
ClinVar RCV Id: RCV003744826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His2572Arg
CA16037976
NM_001354896.2:c.7715A>G