Allele Registry

Canonical Allele Identifier: PA250567

Gene: LHX3 HGNC NCBI

ClinVar RCV:

RCV000009587

ClinVar Variation:

9021

HGVS (amino-acid)	Matching Registered Transcripts
NP_055379.1:p.Tyr116Cys	CA250566 NM_014564.5:c.347A>G