Canonical Allele Identifier: PA2827962204
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His2506Gln
CA16037618
NM_001354897.2:c.7518T>A
CA16037619
NM_001354897.2:c.7518T>G