Canonical Allele Identifier: PA2828028997
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1062362
ClinVar RCV Id: RCV003771188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Glu2296Gly
CA16038130
NM_001354906.2:c.6887A>G