Canonical Allele Identifier: PA2827966502
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411437
ClinVar RCV Id: RCV002230525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln1010Pro
CA16028133
NM_001354898.2:c.3029A>C