Canonical Allele Identifier: PA2825644418
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759598
ClinVar RCV Id: RCV002394098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His2508Gln
CA16037798
NM_001127511.3:c.7524T>A
CA16037799
NM_001127511.3:c.7524T>G