Canonical Allele Identifier: PA2825643950
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 860089
ClinVar RCV Id: RCV003649376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2356Cys
CA16036839
NM_001127511.3:c.7066A>T