Canonical Allele Identifier: PA2825638390
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_001120983.2:p.Leu530Ser
CA16024897
NM_001127511.3:c.1589T>C