Canonical Allele Identifier: PA891852251
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 579289
ClinVar RCV Id: RCV000702532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Gln61Lys
CA378382143
NM_007373.4:c.181C>A