Canonical Allele Identifier: PA2827986827
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1744419
ClinVar RCV Id: RCV002342801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1613Gly
CA16032195
NM_001354900.2:c.4838C>G