Canonical Allele Identifier: PA645400280
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Lys1770Glu
CA041323
NM_001127510.3:c.5308A>G