Canonical Allele Identifier: PA2827998747
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1040272
ClinVar RCV Id: RCV003652188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2463Ala
CA16037772
NM_001354901.2:c.7387C>G