Canonical Allele Identifier: PA2827947617
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759598
ClinVar RCV Id: RCV002394098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.His2526Gln
CA16037798
NM_001354895.2:c.7578T>A
CA16037799
NM_001354895.2:c.7578T>G