Allele Registry

Canonical Allele Identifier: PA102920

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056872

RCV000192114

ClinVar Variation:

66473

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Tyr83His	CA217170 NM_002055.5:c.247T>C