Canonical Allele Identifier: PA2573086974
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331212
ClinVar RCV Id: RCV001806557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro142Ser
CA389475065
NM_005249.5:c.424C>T