Canonical Allele Identifier: PA2827990110
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2816057
ClinVar RCV Id: RCV003744141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val2610Asp
CA16038599
NM_001354900.2:c.7829T>A