Canonical Allele Identifier: PA916042444
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 809782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Val999Ile
CA16028724
NM_001354904.2:c.2995G>A