Canonical Allele Identifier: PA2828007002
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570472
ClinVar RCV Id: RCV003534595

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val1470Ile
CA16032043
NM_001354905.2:c.4408G>A