Canonical Allele Identifier: PA2499270614
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1018957
ClinVar RCV Id: RCV001318323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro108Ser
CA389474862
NM_005249.5:c.322C>T