Canonical Allele Identifier: PA2828023809
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala1652Pro
CA009970
NM_001354903.2:c.4954G>C