Allele Registry

Canonical Allele Identifier: PA102777

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056880

RCV000192120

ClinVar Variation:

66479

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Leu90Pro	CA217184 NM_002055.5:c.269T>C