Canonical Allele Identifier: PA2828053981
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1783048
ClinVar RCV Id: RCV002413175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala487Gly
CA16025556
NM_001354905.2:c.1460C>G