Allele Registry

Canonical Allele Identifier: PA102706

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056882

RCV000192123

RCV003407438

ClinVar Variation:

66481

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Leu101Pro	CA217186 NM_002055.5:c.302T>C