Canonical Allele Identifier: PA2827972223
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg2734His
CA014525
NM_001354898.2:c.8201G>A