Allele Registry

Canonical Allele Identifier: PA106645

Gene: VSX2 HGNC NCBI

ClinVar RCV:

RCV000015986

RCV000015987

RCV000413928

RCV001330573

ClinVar Variation:

14861

HGVS (amino-acid)	Matching Registered Transcripts
NP_878314.1:p.Arg200Pro	CA124413 NM_182894.3:c.599G>C