Canonical Allele Identifier: PA2828028660
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219895
ClinVar RCV Id: RCV000206465 RCV000236866 RCV000570828 RCV003997589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.His2243Arg
CA048553
NM_001354906.2:c.6728A>G