Canonical Allele Identifier: PA2827981764
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135692
ClinVar RCV Id: RCV000122766 RCV000413883 RCV000566722 RCV002228421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg29Gln
CA007680
NM_001354900.2:c.86G>A