Canonical Allele Identifier: PA2827968879
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_001341827.1:p.Lys1719Thr
CA16032764
NM_001354898.2:c.5156A>C