Allele Registry

Canonical Allele Identifier: PA102785

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056881

RCV000192122

ClinVar Variation:

66480

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Leu97Pro	CA217185 NM_002055.5:c.290T>C