Canonical Allele Identifier: PA2827969202
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro1818Thr
CA16033423
NM_001354898.2:c.5452C>A