Canonical Allele Identifier: PA2827950892
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His1072Pro
CA034499
NM_001354896.2:c.3215A>C