Canonical Allele Identifier: PA2573248881
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1510039
ClinVar RCV Id: RCV002011462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Lys147Met
CA389475100
NM_005249.5:c.440A>T