Canonical Allele Identifier: PA2827251005
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2706629
ClinVar RCV Id: RCV003539604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.His113Arg
CA378384297
NM_001324336.2:c.338A>G