Canonical Allele Identifier: PA2828042334
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala1574Thr
CA16032477
NM_001354904.2:c.4720G>A