Canonical Allele Identifier: PA297171
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_031399.2:p.Glu13Ala
CA297169
NM_007373.4:c.38A>C