Canonical Allele Identifier: PA2828008905
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350415
ClinVar Variation Id: 3230807
ClinVar RCV Id: RCV004522921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr1787Ser
CA043197
NM_001354905.2:c.5360C>G
CA16034103
NM_001354905.2:c.5359A>T