Allele Registry

Canonical Allele Identifier: PA102489

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056870

RCV000192111

ClinVar Variation:

66471

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Arg79Pro	CA217168 NM_002055.5:c.236G>C