Canonical Allele Identifier: PA2825024572
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759598
ClinVar RCV Id: RCV002394098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His2526Gln
CA16037798
NM_000038.6:c.7578T>A
CA16037799
NM_000038.6:c.7578T>G