Canonical Allele Identifier: PA2825633429
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1479573
ClinVar RCV Id: RCV003773137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu1683Gly
CA16032370
NM_001127510.3:c.5048A>G