Canonical Allele Identifier: PA131053
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu1317Gln
CA008815
NM_001127510.3:c.3949G>C