Canonical Allele Identifier: PA2828012790
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Lys2612Glu
CA014335
NM_001354902.2:c.7834A>G