Canonical Allele Identifier: PA2826506949
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 573791
ClinVar RCV Id: RCV000695552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Arg24Lys
CA378380927
NM_001269039.3:c.71G>A