Canonical Allele Identifier: PA2827251405
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1749547
ClinVar RCV Id: RCV002359655
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Asp192Glu
CA378386125
NM_001324337.2:c.576T>A
CA378386128
NM_001324337.2:c.576T>G