Canonical Allele Identifier: PA2827998054
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2773592
ClinVar RCV Id: RCV003584448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2253Leu
CA16036458
NM_001354901.2:c.6758C>T