Canonical Allele Identifier: PA2828047819
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759075
ClinVar RCV Id: RCV002391481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Leu2367Ile
CA16037596
NM_001354904.2:c.7099C>A