Canonical Allele Identifier: PA2827250987
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719439
ClinVar RCV Id: RCV002303721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ala88Gly
CA378383196
NM_001324336.2:c.263C>G