Canonical Allele Identifier: PA916040790
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 245782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro1943His
CA042917
NM_001354896.2:c.5828C>A