Canonical Allele Identifier: PA2828054280
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val544Ile
CA007204
NM_001354905.2:c.1630G>A