Canonical Allele Identifier: PA2827250997
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 981610
ClinVar RCV Id: RCV001261151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ser108Cys
CA378384070
NM_001324336.2:c.323C>G