Canonical Allele Identifier: PA2826298209
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 190360
ClinVar RCV Id: RCV000192175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Glu373Ala
CA347228
NM_001242376.3:c.1118A>C