Canonical Allele Identifier: PA2828025330
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Leu1756Phe
CA010933
NM_001354906.2:c.5268G>T
CA16034721
NM_001354906.2:c.5268G>C