Allele Registry

Canonical Allele Identifier: PA916062872

Gene: VSX1 HGNC NCBI

ClinVar RCV:

RCV000304040

RCV000886245

ClinVar Variation:

337962

HGVS (amino-acid)	Matching Registered Transcripts
NP_955457.1:p.Gly160Val	CA9793620 NM_199425.3:c.479G>T