Canonical Allele Identifier: PA2828004156
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759598
ClinVar RCV Id: RCV002394098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His2435Gln
CA16037798
NM_001354902.2:c.7305T>A
CA16037799
NM_001354902.2:c.7305T>G