Canonical Allele Identifier: PA2827970950
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr2354Pro
CA16036870
NM_001354898.2:c.7060A>C