Canonical Allele Identifier: PA2827959843
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 847431
ClinVar RCV Id: RCV002240216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr1783Ala
CA16032958
NM_001354897.2:c.5347A>G