Canonical Allele Identifier: PA2827941604
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Val704Ile
CA007204
NM_001354895.2:c.2110G>A