Canonical Allele Identifier: PA2827976039
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 840675
ClinVar RCV Id: RCV002551518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys1111Glu
CA16028818
NM_001354899.2:c.3331A>G