Allele Registry

Canonical Allele Identifier: PA2828120397

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017559

RCV000056825

ClinVar Variation:

16176

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Glu362Asp	CA217107 NM_001363846.2:c.1086G>C CA399843488 NM_001363846.2:c.1086G>T