Allele Registry

Canonical Allele Identifier: PA2828120386

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017561

RCV000056820

ClinVar Variation:

16178

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Leu352Pro	CA217100 NM_001363846.2:c.1055T>C