Canonical Allele Identifier: PA2825024466
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His2496Gln
CA16037618
NM_000038.6:c.7488T>A
CA16037619
NM_000038.6:c.7488T>G