Canonical Allele Identifier: PA164031
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His1192Tyr
CA008571
NM_001127511.3:c.3574C>T