Canonical Allele Identifier: PA2499276400
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003171
ClinVar RCV Id: RCV001299693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Gly80Arg
CA378382881
NM_007373.4:c.238G>A
CA378382882
NM_007373.4:c.238G>C