Canonical Allele Identifier: PA2827251278
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2795797
ClinVar RCV Id: RCV003655577
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Glu8Gln
CA378380305
NM_001324337.2:c.22G>C