Canonical Allele Identifier: PA2826507196
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_001255968.1:p.Asp192Tyr
CA5689598
NM_001269039.3:c.574G>T