Canonical Allele Identifier: PA645475690
Gene: VSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 314200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878314.1:p.Arg288Gln
CA7266481
NM_182894.3:c.863G>A