Canonical Allele Identifier: PA2827251297
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_001311266.1:p.Glu27Gln
CA378381064
NM_001324337.2:c.79G>C