Canonical Allele Identifier: PA2827940117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141927
ClinVar RCV Id: RCV000130641 RCV003764868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Arg216Gly
CA012188
NM_001354895.2:c.646C>G