Allele Registry

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Canonical Allele Identifier: PA2826507023

Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 561714

ClinVar RCV Id: RCV000681079 RCV000780708

ClinVar Variation Id: 981608

ClinVar RCV Id: RCV001261149 RCV001587301 RCV003655332

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001255968.1:p.Gly63Arg	CA378382243 NM_001269039.3:c.187G>A CA378382246 NM_001269039.3:c.187G>C