Canonical Allele Identifier: PA2826507123
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 632982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Val142Gly
CA5689588
NM_001269039.3:c.425T>G