Allele Registry

Canonical Allele Identifier: PA645381120

Gene: GFAP HGNC NCBI

ClinVar Allele:

361017

ClinVar RCV:

RCV000415341

ClinVar Variation:

374003

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Tyr349Ser	CA16043529 NM_002055.5:c.1046A>C