Canonical Allele Identifier: PA2825642003
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746238
ClinVar RCV Id: RCV002344319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Lys1726Thr
CA16032764
NM_001127511.3:c.5177A>C