Canonical Allele Identifier: PA2580319410
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773061
ClinVar RCV Id: RCV002394717

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro486Ser
CA389477304
NM_005249.5:c.1456C>T