Canonical Allele Identifier: PA2828011426
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly2202Ala
CA16036765
NM_001354905.2:c.6605G>C