Canonical Allele Identifier: PA1139733407
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469795
ClinVar RCV Id: RCV003537039
ClinVar Variation Id: 1371388
ClinVar RCV Id: RCV003772618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly23Arg
CA124925142
NM_001354902.2:c.67G>A
CA360611835
NM_001354902.2:c.67G>C