Canonical Allele Identifier: PA2580369035
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1786700
ClinVar RCV Id: RCV002432420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Ile72Val
CA378382592
NM_007373.4:c.214A>G