Allele Registry

Canonical Allele Identifier: PA217142

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056849

RCV000192186

ClinVar Variation:

66454

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Asp417Ala	CA217141 NM_002055.5:c.1250A>C