Canonical Allele Identifier: PA2827958241
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr1302Met
CA008722
NM_001354897.2:c.3905C>T