Canonical Allele Identifier: PA2828047834
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2792114
ClinVar RCV Id: RCV003745801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2369Ala
CA16037607
NM_001354904.2:c.7105A>G