Canonical Allele Identifier: PA1139703267
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 704508
ClinVar Variation Id: 1790283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro80del
CA258396552
NM_005249.5:c.234_236del
CA961450348
NM_005249.5:c.237_239del