Canonical Allele Identifier: PA2825774496
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 16177
ClinVar RCV Id: RCV000017560 RCV000056910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Arg276Leu
CA217223
NM_001131019.3:c.827G>T