Canonical Allele Identifier: PA891852248
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 573791
ClinVar RCV Id: RCV000695552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Arg24Lys
CA378380927
NM_007373.4:c.71G>A