Canonical Allele Identifier: PA136659
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40635
ClinVar RCV Id: RCV000038777 RCV000518991 RCV000680308 RCV001286384 RCV003914899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Ser4Arg
CA136657
NM_007373.4:c.10A>C
CA378380180
NM_007373.4:c.12T>A
CA378380183
NM_007373.4:c.12T>G