Allele Registry

Canonical Allele Identifier: PA094963

Gene: VSX1 HGNC NCBI

ClinVar RCV:

RCV000005562

RCV002247253

ClinVar Variation:

5250

HGVS (amino-acid)	Matching Registered Transcripts
NP_055403.2:p.Ala256Ser	CA117358 NM_014588.6:c.766G>T