Canonical Allele Identifier: PA916040501
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile1708Val
CA040590
NM_001354896.2:c.5122A>G