Canonical Allele Identifier: PA2827985368
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.His1169Tyr
CA008571
NM_001354900.2:c.3505C>T