Canonical Allele Identifier: PA916039697
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Leu674Val
CA030483
NM_001354896.2:c.2020C>G