Canonical Allele Identifier: PA2828020759
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Glu1216Gln
CA008815
NM_001354903.2:c.3646G>C