Canonical Allele Identifier: PA2580319170
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2413593
ClinVar RCV Id: RCV003104389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly148Ala
CA389475108
NM_005249.5:c.443G>C