Allele Registry

Canonical Allele Identifier: PA106630

Gene: VSX2 HGNC NCBI

ClinVar RCV:

RCV000015985

RCV001851882

ClinVar Variation:

14860

HGVS (amino-acid)	Matching Registered Transcripts
NP_878314.1:p.Arg200Gln	CA124412 NM_182894.3:c.599G>A