Canonical Allele Identifier: PA2828025078
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_001341832.1:p.Thr1846Ser
CA043197
NM_001354903.2:c.5537C>G
CA16034103
NM_001354903.2:c.5536A>T