Canonical Allele Identifier: PA645400744
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 245782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1925His
CA042917
NM_001127510.3:c.5774C>A