Canonical Allele Identifier: PA2827995877
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro1589His
CA16032155
NM_001354901.2:c.4766C>A