Canonical Allele Identifier: PA2827953671
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val124Ile
CA16022128
NM_001354896.2:c.370G>A