Canonical Allele Identifier: PA658723049
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496405
ClinVar RCV Id: RCV000587719
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Glu37Gln
CA378381409
NM_007373.4:c.109G>C