Canonical Allele Identifier: PA2827250918
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2640834
ClinVar RCV Id: RCV003422881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ser4Asn
CA378380168
NM_001324336.2:c.11G>A