Allele Registry

Canonical Allele Identifier: PA916044549

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017552

RCV000056848

RCV001267511

ClinVar Variation:

16169

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Arg456Trp	CA217140 NM_001363846.2:c.1366C>T