Allele Registry

Canonical Allele Identifier: PA2825774479

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056904

RCV000192140

ClinVar Variation:

66501

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Ser247Pro	CA217215 NM_001131019.3:c.739T>C