Allele Registry

Canonical Allele Identifier: PA891850220

Gene: FOXG1 HGNC NCBI

ClinVar RCV:

RCV000701355

ClinVar Variation:

578372

HGVS (amino-acid)	Matching Registered Transcripts
NP_005240.3:p.Ser185Thr	CA389475349 NM_005249.5:c.554G>C