Canonical Allele Identifier: PA2826506986
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2076274
ClinVar RCV Id: RCV002979194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Glu37Gly
CA378381447
NM_001269039.3:c.110A>G