Canonical Allele Identifier: PA913198104
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 632982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Val142Gly
CA5689588
NM_007373.4:c.425T>G