Canonical Allele Identifier: PA2828003819
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly2212Arg
CA012645
NM_001354902.2:c.6634G>A
CA16036399
NM_001354902.2:c.6634G>C