Allele Registry

Canonical Allele Identifier: PA102898

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056907

RCV000192142

ClinVar Variation:

66504

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Tyr257Cys	CA217220 NM_002055.5:c.770A>G