Canonical Allele Identifier: PA2827251051
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1749638
ClinVar RCV Id: RCV002359746

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ser193Cys
CA378386141
NM_001324336.2:c.578C>G