Canonical Allele Identifier: PA2827250933
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 652343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Val18Ile
CA378380699
NM_001324336.2:c.52G>A