Canonical Allele Identifier: PA916079263
Gene: VSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 660623
ClinVar RCV Id: RCV000817859 RCV001830794
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878314.1:p.Ser213Asn
CA390369246
NM_182894.3:c.638G>A