Canonical Allele Identifier: PA2828027427
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2773592
ClinVar RCV Id: RCV003584448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro2211Leu
CA16036458
NM_001354903.2:c.6632C>T