Canonical Allele Identifier: PA2741919985
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3015649
ClinVar RCV Id: RCV003873736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro139Ser
CA389475047
NM_005249.5:c.415C>T