Canonical Allele Identifier: PA1139736052
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 935079
ClinVar RCV Id: RCV001203590 RCV001261148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Glu27Gln
CA378381064
NM_007373.4:c.79G>C