Canonical Allele Identifier: PA2828012665
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628704
ClinVar RCV Id: RCV000773365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2392Gly
CA16037959
NM_001354905.2:c.7174A>G