Allele Registry

Canonical Allele Identifier: PA105984

Gene: LHX3 HGNC NCBI

ClinVar RCV:

RCV000009587

ClinVar Variation:

9021

HGVS (amino-acid)	Matching Registered Transcripts
NP_835258.1:p.Tyr111Cys	CA250566 NM_178138.6:c.332A>G