Canonical Allele Identifier: PA2828001777
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Glu1118Lys
CA008564
NM_001354902.2:c.3352G>A