Canonical Allele Identifier: PA2827986950
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745225
ClinVar RCV Id: RCV002335894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly1653Asp
CA16032440
NM_001354900.2:c.4958G>A