Canonical Allele Identifier: PA2827250936
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 573791
ClinVar RCV Id: RCV000695552
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Arg24Lys
CA378380927
NM_001324336.2:c.71G>A