Canonical Allele Identifier: PA2828053305
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566964
ClinVar RCV Id: RCV003306834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser392Pro
CA16024924
NM_001354905.2:c.1174T>C