Canonical Allele Identifier: PA2827951149
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2852532
ClinVar RCV Id: RCV003743093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1151Gly
CA16028780
NM_001354896.2:c.3452A>G