Canonical Allele Identifier: PA2827996487
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val1775Ile
CA042161
NM_001354901.2:c.5323G>A