Canonical Allele Identifier: PA2827251078
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 298860
ClinVar RCV Id: RCV000367311
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ile234Thr
CA5689611
NM_001324336.2:c.701T>C