Canonical Allele Identifier: PA2826506987
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496405
ClinVar RCV Id: RCV000587719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Glu37Gln
CA378381409
NM_001269039.3:c.109G>C