Canonical Allele Identifier: PA2827250959
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2014740
ClinVar RCV Id: RCV002861632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Thr45Ser
CA378381708
NM_001324336.2:c.133A>T
CA378381718
NM_001324336.2:c.134C>G