Canonical Allele Identifier: PA314595
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205477
ClinVar RCV Id: RCV000187447 RCV001206355 RCV001704987 RCV002444758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Met426Ile
CA314594
NM_005249.5:c.1278G>A
CA389476918
NM_005249.5:c.1278G>C
CA389476919
NM_005249.5:c.1278G>T