Canonical Allele Identifier: PA2827969462
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 245782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro1900His
CA042917
NM_001354898.2:c.5699C>A