Canonical Allele Identifier: PA658671324
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448933
ClinVar RCV Id: RCV000521093
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Thr205Ala
CA5689601
NM_007373.4:c.613A>G