Canonical Allele Identifier: PA2741919988
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504016
ClinVar RCV Id: RCV003231007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Lys147Arg
CA389475101
NM_005249.5:c.440A>G