Canonical Allele Identifier: PA2828033290
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1777096
ClinVar RCV Id: RCV002403589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Leu422Ser
CA16024897
NM_001354904.2:c.1265T>C