Canonical Allele Identifier: PA297177
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Ile119Val
CA297175
NM_007373.4:c.355A>G