Canonical Allele Identifier: PA2827993426
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232412
ClinVar Variation Id: 663857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gly848Arg
CA033124
NM_001354901.2:c.2542G>A
CA033134
NM_001354901.2:c.2542G>C