Allele Registry

Canonical Allele Identifier: PA100996

Gene: FOXG1 HGNC NCBI

ClinVar RCV:

RCV000170082

ClinVar Variation:

189620

HGVS (amino-acid)	Matching Registered Transcripts
NP_005240.3:p.Arg244Cys	CA199444 NM_005249.5:c.730C>T