Allele Registry

Canonical Allele Identifier: PA347227

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000192164

ClinVar Variation:

190358

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Ala364Thr	CA347226 NM_002055.5:c.1090G>A