Canonical Allele Identifier: PA2580369013
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2265459
ClinVar RCV Id: RCV004120669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Ser2Thr
CA378380117
NM_007373.4:c.5G>C