Canonical Allele Identifier: PA2826297917
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 323628
ClinVar RCV Id: RCV000996566 RCV002521111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Val15Ile
CA8609123
NM_001242376.3:c.43G>A