Canonical Allele Identifier: PA2580369014
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717401
ClinVar RCV Id: RCV002297589
ClinVar Variation Id: 3061176
ClinVar RCV Id: RCV003982688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Gly6Arg
CA378380211
NM_007373.4:c.16G>A
CA378380219
NM_007373.4:c.16G>C