Canonical Allele Identifier: PA2828006400
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr1333Met
CA009574
NM_001354905.2:c.3998C>T