Canonical Allele Identifier: PA2825638398
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566964
ClinVar RCV Id: RCV003306834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser534Pro
CA16024924
NM_001127511.3:c.1600T>C