Canonical Allele Identifier: PA164033
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His1210Tyr
CA008571
NM_001127510.3:c.3628C>T