Canonical Allele Identifier: PA2828041284
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1369536
ClinVar RCV Id: RCV001870683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr1459Ala
CA16031754
NM_001354904.2:c.4375A>G