Canonical Allele Identifier: PA2827994432
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His1151Tyr
CA008571
NM_001354901.2:c.3451C>T