Canonical Allele Identifier: PA2828042917
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys1644Glu
CA041323
NM_001354904.2:c.4930A>G