Canonical Allele Identifier: PA2827970703
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly2278Arg
CA012645
NM_001354898.2:c.6832G>A
CA16036399
NM_001354898.2:c.6832G>C