Canonical Allele Identifier: PA2827954268
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_001341826.1:p.Gly23Arg
CA124925142
NM_001354897.2:c.67G>A
CA360611835
NM_001354897.2:c.67G>C