Canonical Allele Identifier: PA2827985098
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629986
ClinVar RCV Id: RCV000774851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp1093Gly
CA16028788
NM_001354900.2:c.3278A>G