Canonical Allele Identifier: PA2827966110
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.His888Arg
CA033216
NM_001354898.2:c.2663A>G