Canonical Allele Identifier: PA645455645
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_031399.2:p.Ile234Thr
CA5689611
NM_007373.4:c.701T>C