Canonical Allele Identifier: PA2580369052
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1746510
ClinVar RCV Id: RCV002344399 RCV003776076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Leu176Ile
CA378385834
NM_007373.4:c.526T>A