Canonical Allele Identifier: PA2827251360
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 950431
ClinVar RCV Id: RCV001222137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Ile112Val
CA378384258
NM_001324337.2:c.334A>G