Allele Registry

Canonical Allele Identifier: PA2580529548

Gene: LNX2 HGNC NCBI

ClinVar RCV:

RCV004152782

ClinVar Variation:

2304211

HGVS (amino-acid)	Matching Registered Transcripts
NP_699202.1:p.Gly205Ser	CA6927082 NM_153371.4:c.613G>A