Allele Registry

Canonical Allele Identifier: PA094972

Gene: VSX1 HGNC NCBI

ClinVar RCV:

RCV000005559

RCV001140683

ClinVar Variation:

5247

HGVS (amino-acid)	Matching Registered Transcripts
NP_055403.2:p.Arg166Trp	CA117354 NM_014588.6:c.496C>T