Canonical Allele Identifier: PA2825774488
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 190346
ClinVar RCV Id: RCV000192145
ClinVar Variation Id: 190347
ClinVar RCV Id: RCV000192146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Leu264Pro
CA347206
NM_001131019.3:c.791T>C
CA347208
NM_001131019.3:c.791_792delinsCT