Canonical Allele Identifier: PA916040722
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1889Tyr
CA042401
NM_001354896.2:c.5665G>T