Canonical Allele Identifier: PA2828044323
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127309
ClinVar Variation Id: 141168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro1834Leu
CA010751
NM_001354904.2:c.5501_5502delinsTA
CA010760
NM_001354904.2:c.5501C>T