Allele Registry

Canonical Allele Identifier: PA2828120394

Gene: GFAP HGNC NCBI

ClinVar Allele:

77328

ClinVar RCV:

RCV000056824

RCV000192162

ClinVar Variation:

66431

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Asp360Val	CA217105 NM_001363846.2:c.1079A>T