Canonical Allele Identifier: PA1139703439
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 957393
ClinVar RCV Id: RCV001230364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro109Thr
CA389474868
NM_005249.5:c.325C>A