Canonical Allele Identifier: PA2827945306
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 21030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Val1822Asp
CA010422
NM_001354895.2:c.5465T>A