Canonical Allele Identifier: PA2741920066
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2837204
ClinVar RCV Id: RCV003630669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ser472Thr
CA389477204
NM_005249.5:c.1414T>A