Canonical Allele Identifier: PA2573248871
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1364474
ClinVar RCV Id: RCV001942421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Asp96Ala
CA389474786
NM_005249.5:c.287A>C