Canonical Allele Identifier: PA2827989594
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.His2455Gln
CA16037618
NM_001354900.2:c.7365T>A
CA16037619
NM_001354900.2:c.7365T>G