ClinGen Allele Registry
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Canonical Allele Identifier:
PA238811
Gene: FOXG1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
193306
ClinVar RCV Id:
RCV000173367
RCV000648323
RCV000724697
RCV002426828
RCV003448278
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005240.3:p.Gln73Pro
CA238810
NM_005249.5:c.218A>C