Canonical Allele Identifier: PA645400785
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_001120982.1:p.Thr1947Ser
CA043197
NM_001127510.3:c.5840C>G
CA16034103
NM_001127510.3:c.5839A>T