Canonical Allele Identifier: PA2828002466
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1720459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Glu1469Lys
CA16031584
NM_001354902.2:c.4405G>A