Canonical Allele Identifier: PA2827985716
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Glu1276Gln
CA008815
NM_001354900.2:c.3826G>C