Canonical Allele Identifier: PA2827251058
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 240838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ile204Val
CA5689600
NM_001324336.2:c.610A>G