Canonical Allele Identifier: PA2827968619
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 653217
ClinVar RCV Id: RCV002537302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu1643Gly
CA16032280
NM_001354898.2:c.4928A>G