Canonical Allele Identifier: PA2499270613
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1195165
ClinVar RCV Id: RCV001558146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Leu102Pro
CA389474830
NM_005249.5:c.305T>C