Canonical Allele Identifier: PA234032
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 167090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro80dup
CA234031
NM_005249.5:c.234_236dup
CA2624398586
NM_005249.5:c.237_239dup