Canonical Allele Identifier: PA2827960399
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1406039
ClinVar RCV Id: RCV003772772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala1956Glu
CA16034099
NM_001354897.2:c.5867C>A