Canonical Allele Identifier: PA2827946911
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2773592
ClinVar RCV Id: RCV003584448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro2312Leu
CA16036458
NM_001354895.2:c.6935C>T