Canonical Allele Identifier: PA658807230
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 516265
ClinVar RCV Id: RCV000612307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro112Leu
CA389474888
NM_005249.5:c.335C>T