Canonical Allele Identifier: PA2826507037
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1786700
ClinVar RCV Id: RCV002432420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ile72Val
CA378382592
NM_001269039.3:c.214A>G