Canonical Allele Identifier: PA2828028861
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2273Leu
CA048890
NM_001354906.2:c.6818C>T