Canonical Allele Identifier: PA2828120413
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1306407
ClinVar RCV Id: RCV001767361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Gly372Asp
CA291028407
NM_001363846.2:c.1115G>A