Canonical Allele Identifier: PA916040075
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile1325Lys
CA008761
NM_001354896.2:c.3974T>A