Allele Registry

Canonical Allele Identifier: PA2826298173

Gene: GFAP HGNC NCBI

ClinVar Allele:

1304652

ClinVar RCV:

RCV001772900

ClinVar Variation:

1314391

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229305.1:p.Tyr349Cys	CA399843763 NM_001242376.3:c.1046A>G