ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA172192
Gene: FOXG1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
158598
ClinVar RCV Id:
RCV000145994
RCV000170083
RCV001260760
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005240.3:p.Gly252Val
CA172191
NM_005249.5:c.755G>T