Canonical Allele Identifier: PA172200
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 158602
ClinVar RCV Id: RCV000145998 RCV000480864 RCV001507048
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly267Ser
CA172199
NM_005249.5:c.799G>A