Canonical Allele Identifier: PA2827998465
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg2380His
CA16037262
NM_001354901.2:c.7139G>A