Canonical Allele Identifier: PA915992981
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 682309
ClinVar RCV Id: RCV000842369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Cys396Ser
CA389476717
NM_005249.5:c.1186T>A
CA389476721
NM_005249.5:c.1187G>C