Canonical Allele Identifier: PA2825642628
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_001120983.2:p.Thr1929Ser
CA043197
NM_001127511.3:c.5786C>G
CA16034103
NM_001127511.3:c.5785A>T