Canonical Allele Identifier: PA2827967465
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu1292Gln
CA008815
NM_001354898.2:c.3874G>C