Canonical Allele Identifier: PA2828120119
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1416421
ClinVar RCV Id: RCV001921246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Arg11His
CA8609128
NM_001363846.2:c.32G>A