Canonical Allele Identifier: PA2828049571
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1722068
ClinVar RCV Id: RCV003743930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Val2622Ile
CA16039216
NM_001354904.2:c.7864G>A