Canonical Allele Identifier: PA2825021143
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1446639
ClinVar RCV Id: RCV003653542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro1648Leu
CA16032157
NM_000038.6:c.4943C>T