Canonical Allele Identifier: PA2828013052
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3071818
ClinVar RCV Id: RCV004016312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Lys2456Glu
CA16038378
NM_001354905.2:c.7366A>G