Canonical Allele Identifier: PA172194
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 158599
ClinVar RCV Id: RCV000145995
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Asn253Asp
CA172193
NM_005249.5:c.757A>G