Canonical Allele Identifier: PA2827995598
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1720459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Glu1501Lys
CA16031584
NM_001354901.2:c.4501G>A