Canonical Allele Identifier: PA2828028400
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2773631
ClinVar RCV Id: RCV003584487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro2203Leu
CA16037559
NM_001354906.2:c.6608C>T