Canonical Allele Identifier: PA2827943554
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr1292Met
CA008722
NM_001354895.2:c.3875C>T