Canonical Allele Identifier: PA347213
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 190350
ClinVar RCV Id: RCV000192150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Gln290Glu
CA347212
NM_002055.5:c.868C>G