Canonical Allele Identifier: PA2826507192
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1896072
ClinVar RCV Id: RCV002571854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Arg190Gly
CA378386076
NM_001269039.3:c.568A>G