Canonical Allele Identifier: PA2573086972
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1304019
ClinVar RCV Id: RCV001758312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro69Leu
CA389474627
NM_005249.5:c.206C>T