Canonical Allele Identifier: PA2825774508
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 190350
ClinVar RCV Id: RCV000192150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Gln290Glu
CA347212
NM_001131019.3:c.868C>G