Canonical Allele Identifier: PA2827251329
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784741
ClinVar RCV Id: RCV002419770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Val68Ile
CA378382452
NM_001324337.2:c.202G>A