Canonical Allele Identifier: PA2827251276
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717401
ClinVar RCV Id: RCV002297589
ClinVar Variation Id: 3061176
ClinVar RCV Id: RCV003982688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Gly6Arg
CA378380211
NM_001324337.2:c.16G>A
CA378380219
NM_001324337.2:c.16G>C