Canonical Allele Identifier: PA891850168
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 589083
ClinVar RCV Id: RCV002318026
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro79Ser
CA389474686
NM_005249.5:c.235C>T