Canonical Allele Identifier: PA2827250954
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496405
ClinVar RCV Id: RCV000587719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Glu37Gln
CA378381409
NM_001324336.2:c.109G>C