Canonical Allele Identifier: PA2826506965
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1321351
ClinVar RCV Id: RCV001779445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Lys29Glu
CA378381171
NM_001269039.3:c.85A>G