Canonical Allele Identifier: PA2828034119
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Leu536Ile
CA030573
NM_001354904.2:c.1606C>A