Canonical Allele Identifier: PA2827968969
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Lys1745Glu
CA041323
NM_001354898.2:c.5233A>G