Canonical Allele Identifier: PA314632
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205497
ClinVar RCV Id: RCV000428947 RCV001210916
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ser349Ala
CA314631
NM_005249.5:c.1045T>G