Canonical Allele Identifier: PA2827251309
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2076274
ClinVar RCV Id: RCV002979194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Glu37Gly
CA378381447
NM_001324337.2:c.110A>G