Canonical Allele Identifier: PA2827966808
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln1098Pro
CA008326
NM_001354898.2:c.3293A>C