Canonical Allele Identifier: PA2827250971
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_001311265.1:p.Gly63Arg
CA378382243
NM_001324336.2:c.187G>A
CA378382246
NM_001324336.2:c.187G>C