Canonical Allele Identifier: PA658677821
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 452682
ClinVar RCV Id: RCV000522911 RCV001297654 RCV003235269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Met191Ile
CA389475390
NM_005249.5:c.573G>A
CA389475391
NM_005249.5:c.573G>C
CA389475392
NM_005249.5:c.573G>T