Allele Registry

Canonical Allele Identifier: PA2825774543

Gene: GFAP HGNC NCBI

ClinVar Allele:

1304652

ClinVar RCV:

RCV001772900

ClinVar Variation:

1314391

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124491.1:p.Tyr349Cys	CA399843763 NM_001131019.3:c.1046A>G