Canonical Allele Identifier: PA2827250998
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1493406
ClinVar RCV Id: RCV002012633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Lys109Arg
CA378384107
NM_001324336.2:c.326A>G