Canonical Allele Identifier: PA2827945751
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127309
ClinVar Variation Id: 141168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro1960Leu
CA010751
NM_001354895.2:c.5879_5880delinsTA
CA010760
NM_001354895.2:c.5879C>T