Canonical Allele Identifier: PA2828002003
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Glu1226Gln
CA008815
NM_001354902.2:c.3676G>C