Allele Registry

Canonical Allele Identifier: PA916044546

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056847

RCV000192184

ClinVar Variation:

66453

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Ser438Tyr	CA217138 NM_001363846.2:c.1313C>A