Canonical Allele Identifier: PA1139736328
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 948626
ClinVar RCV Id: RCV001219923 RCV002484194 RCV004032377
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Val207Met
CA213257079
NM_007373.4:c.619G>A