Canonical Allele Identifier: PA2828024843
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127309
ClinVar Variation Id: 141168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro1677Leu
CA010751
NM_001354906.2:c.5030_5031delinsTA
CA010760
NM_001354906.2:c.5030C>T