Canonical Allele Identifier: PA2573258007
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1467895
ClinVar RCV Id: RCV001993521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Leu176Ser
CA378385839
NM_007373.4:c.527T>C