Canonical Allele Identifier: PA2827950755
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2734199
ClinVar RCV Id: RCV003535146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser1028Cys
CA16027956
NM_001354896.2:c.3082A>T