Canonical Allele Identifier: PA2825774581
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 590968
ClinVar RCV Id: RCV000722139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Asn375Lys
CA399843303
NM_001131019.3:c.1125C>G
CA399843304
NM_001131019.3:c.1125C>A