Canonical Allele Identifier: PA2828009704
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Lys1679Glu
CA041323
NM_001354902.2:c.5035A>G