Canonical Allele Identifier: PA2499270633
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1165214
ClinVar RCV Id: RCV001512110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro419Ser
CA389476869
NM_005249.5:c.1255C>T