Canonical Allele Identifier: PA2825643762
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2773592
ClinVar RCV Id: RCV003584448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2294Leu
CA16036458
NM_001127511.3:c.6881C>T