Canonical Allele Identifier: PA2828025193
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127309
ClinVar Variation Id: 141168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro1859Leu
CA010751
NM_001354903.2:c.5576_5577delinsTA
CA010760
NM_001354903.2:c.5576C>T