Canonical Allele Identifier: PA916041056
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470050
ClinVar RCV Id: RCV002358548 RCV003470762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2188Ser
CA16035571
NM_001354896.2:c.6562C>T