Allele Registry

Canonical Allele Identifier: PA314589

Gene: FOXG1 HGNC NCBI

ClinVar RCV:

RCV000187444

RCV000540363

RCV001507039

RCV001704986

RCV002317097

RCV003947570

ClinVar Variation:

205474

HGVS (amino-acid)	Matching Registered Transcripts
NP_005240.3:p.Gly168Ala	CA314588 NM_005249.5:c.503G>C