Canonical Allele Identifier: PA2828022481
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_001341835.1:p.Thr1302Ala
CA16031754
NM_001354906.2:c.3904A>G