Canonical Allele Identifier: PA2827998089
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2115874
ClinVar RCV Id: RCV003744952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gln2263Glu
CA16036519
NM_001354901.2:c.6787C>G