Canonical Allele Identifier: PA2826506954
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Glu25Gly
CA297172
NM_001269039.3:c.74A>G