Canonical Allele Identifier: PA2827994795
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val1261Glu
CA037191
NM_001354901.2:c.3782T>A