Allele Registry

Canonical Allele Identifier: PA172198

Gene: FOXG1 HGNC NCBI

ClinVar RCV:

RCV000145997

RCV003883314

ClinVar Variation:

158601

3024268

HGVS (amino-acid)	Matching Registered Transcripts
NP_005240.3:p.Trp255Cys	CA172197 NM_005249.5:c.765G>T CA389475821 NM_005249.5:c.765G>C