Canonical Allele Identifier: PA314625
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205493
ClinVar RCV Id: RCV000187466 RCV000803740
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly271Asp
CA314624
NM_005249.5:c.812G>A