Canonical Allele Identifier: PA2825630408
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3229472
ClinVar RCV Id: RCV004525050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1140Ser
CA16028827
NM_001127510.3:c.3418C>T