Canonical Allele Identifier: PA2828008158
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 21030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val1662Asp
CA010422
NM_001354905.2:c.4985T>A