Canonical Allele Identifier: PA2827250966
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2079868
ClinVar RCV Id: RCV002998850 RCV003170804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ser58Asn
CA5689560
NM_001324336.2:c.173G>A