Canonical Allele Identifier: PA2828022997
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Glu1390Gly
CA16032310
NM_001354906.2:c.4169A>G