Canonical Allele Identifier: PA916042218
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp266Glu
CA16023011
NM_001354902.2:c.798T>A
CA16023012
NM_001354902.2:c.798T>G