Allele Registry

Canonical Allele Identifier: PA891850168

Gene: FOXG1 HGNC NCBI

ClinVar Allele:

579952

ClinVar RCV:

RCV002318026

ClinVar Variation:

589083

HGVS (amino-acid)	Matching Registered Transcripts
NP_005240.3:p.Pro79Ser	CA389474686 NM_005249.5:c.235C>T