Canonical Allele Identifier: PA2828002870
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala1662Pro
CA009970
NM_001354902.2:c.4984G>C