Canonical Allele Identifier: PA2827251019
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 632982
ClinVar RCV Id: RCV000780709 RCV003655210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Val142Gly
CA5689588
NM_001324336.2:c.425T>G