Canonical Allele Identifier: PA2827251300
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2804581
ClinVar RCV Id: RCV003655636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Ala30Thr
CA378381206
NM_001324337.2:c.88G>A