Canonical Allele Identifier: PA2826507161
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1955903
ClinVar RCV Id: RCV002695739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Arg172Gln
CA378385780
NM_001269039.3:c.515G>A