Canonical Allele Identifier: PA2825015607
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566964
ClinVar RCV Id: RCV003306834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser552Pro
CA16024924
NM_000038.6:c.1654T>C