Canonical Allele Identifier: PA2828042766
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala1627Pro
CA009970
NM_001354904.2:c.4879G>C