Canonical Allele Identifier: PA2827996855
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_001341830.1:p.Thr1888Ser
CA043197
NM_001354901.2:c.5663C>G
CA16034103
NM_001354901.2:c.5662A>T