Canonical Allele Identifier: PA916040492
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 657857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gln1698Glu
CA040478
NM_001354896.2:c.5092C>G