Canonical Allele Identifier: PA1139740026
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 847431
ClinVar RCV Id: RCV002240216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr1791Ala
CA16032958
NM_001354896.2:c.5371A>G