Canonical Allele Identifier: PA2741935657
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2906236
ClinVar RCV Id: RCV003654773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Thr195Ile
CA378386171
NM_007373.4:c.584C>T