Canonical Allele Identifier: PA2828002671
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Glu1572Lys
CA040323
NM_001354902.2:c.4714G>A