Canonical Allele Identifier: PA2573089801
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1309835
ClinVar RCV Id: RCV001756903 RCV001868457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Asp192Tyr
CA5689598
NM_007373.4:c.574G>T