Canonical Allele Identifier: PA658807325
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 522167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro419Leu
CA389476872
NM_005249.5:c.1256C>T