Canonical Allele Identifier: PA2828007794
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala1593Pro
CA009970
NM_001354905.2:c.4777G>C