Canonical Allele Identifier: PA2573257997
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1493406
ClinVar RCV Id: RCV002012633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Lys109Arg
CA378384107
NM_007373.4:c.326A>G