Canonical Allele Identifier: PA2741935604
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2795797
ClinVar RCV Id: RCV003655577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Glu8Gln
CA378380305
NM_007373.4:c.22G>C