Allele Registry

Canonical Allele Identifier: PA217139

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056847

RCV000192184

ClinVar Variation:

66453

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Ser398Tyr	CA217138 NM_002055.5:c.1193C>A