Canonical Allele Identifier: PA2827962366
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 924804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly2555Arg
CA16037909
NM_001354897.2:c.7663G>A
CA16037910
NM_001354897.2:c.7663G>C