Canonical Allele Identifier: PA2828007906
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Lys1610Glu
CA041323
NM_001354905.2:c.4828A>G