Canonical Allele Identifier: PA2828023676
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val1493Ile
CA041569
NM_001354906.2:c.4477G>A