Canonical Allele Identifier: PA163863
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala1735Pro
CA009970
NM_001127511.3:c.5203G>C