Canonical Allele Identifier: PA2573248895
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372241
ClinVar RCV Id: RCV001872836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Thr298Ser
CA389476083
NM_005249.5:c.892A>T
CA389476085
NM_005249.5:c.893C>G