Canonical Allele Identifier: PA2828009322
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_001341831.1:p.Pro1557Leu
CA16032157
NM_001354902.2:c.4670C>T