Canonical Allele Identifier: PA101004
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13870
ClinVar RCV Id: RCV000014884
ClinVar Variation Id: 373043
ClinVar RCV Id: RCV000414314 RCV001069733
ClinVar Variation Id: 1068106
ClinVar RCV Id: RCV001379557
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Phe215Leu
CA123554
NM_005249.5:c.643T>C
CA16042954
NM_005249.5:c.645C>G
CA389475558
NM_005249.5:c.645C>A