Canonical Allele Identifier: PA2827250929
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181526
ClinVar RCV Id: RCV000159108 RCV000519096 RCV001286466 RCV003917545
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Glu13Ala
CA297169
NM_001324336.2:c.38A>C