Canonical Allele Identifier: PA645475679
Gene: VSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 314194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878314.1:p.Arg178Gln
CA10646003
NM_182894.3:c.533G>A