Allele Registry

Canonical Allele Identifier: PA101004

Gene: FOXG1 HGNC NCBI

ClinVar RCV:

RCV000014884

RCV000414314

RCV001069733

RCV001379557

ClinVar Variation:

13870

373043

1068106

HGVS (amino-acid)	Matching Registered Transcripts
NP_005240.3:p.Phe215Leu	CA123554 NM_005249.5:c.643T>C CA16042954 NM_005249.5:c.645C>G CA389475558 NM_005249.5:c.645C>A