Canonical Allele Identifier: PA218977
Gene: VSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 68079
ClinVar RCV Id: RCV000058885 RCV000673950
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878314.1:p.Gly289Asp
CA218976
NM_182894.3:c.866G>A