Canonical Allele Identifier: PA2827965169
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127278
ClinVar RCV Id: RCV000115070 RCV000198802 RCV000417366 RCV000679049 RCV001353927 RCV003743561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Val584Ile
CA006055
NM_001354898.2:c.1750G>A