Canonical Allele Identifier: PA2827250984
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2450870
ClinVar RCV Id: RCV003171525
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ser86Gly
CA378383080
NM_001324336.2:c.256A>G