Canonical Allele Identifier: PA2827250991
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2450868
ClinVar RCV Id: RCV003177264
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Cys97Phe
CA378383628
NM_001324336.2:c.290G>T