Canonical Allele Identifier: PA2827980553
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231322
ClinVar RCV Id: RCV004525393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys2478Thr
CA16037672
NM_001354899.2:c.7433A>C