Canonical Allele Identifier: PA2827959691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3014066
ClinVar RCV Id: RCV003875705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala1741Val
CA16032680
NM_001354897.2:c.5222C>T