Allele Registry

Canonical Allele Identifier: PA102542

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017558

RCV000056864

ClinVar Variation:

16175

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Asn77Tyr	CA217161 NM_002055.5:c.229A>T