Canonical Allele Identifier: PA2825630391
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1507413
ClinVar RCV Id: RCV003773388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu1136Gly
CA16028800
NM_001127510.3:c.3407A>G