Canonical Allele Identifier: PA163864
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1753Pro
CA009970
NM_000038.6:c.5257G>C