Canonical Allele Identifier: PA2828035832
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232412
ClinVar Variation Id: 663857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gly781Arg
CA033124
NM_001354904.2:c.2341G>A
CA033134
NM_001354904.2:c.2341G>C