Canonical Allele Identifier: PA2827964527
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1023938
ClinVar RCV Id: RCV003770760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Lys373Glu
CA16023915
NM_001354898.2:c.1117A>G