Allele Registry

Canonical Allele Identifier: PA347213

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000192150

ClinVar Variation:

190350

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