Canonical Allele Identifier: PA2827998658
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His2437Gln
CA16037618
NM_001354901.2:c.7311T>A
CA16037619
NM_001354901.2:c.7311T>G