Canonical Allele Identifier: PA2827967114
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.His1185Tyr
CA008571
NM_001354898.2:c.3553C>T