Canonical Allele Identifier: PA2828043450
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro1717Thr
CA16033423
NM_001354904.2:c.5149C>A