Canonical Allele Identifier: PA2828011628
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr2265Ala
CA046771
NM_001354902.2:c.6793A>G