Canonical Allele Identifier: PA2827251043
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1748749
ClinVar RCV Id: RCV002345078 RCV003539427
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Val188Leu
CA378386042
NM_001324336.2:c.562G>T
CA378386044
NM_001324336.2:c.562G>C