Allele Registry

Canonical Allele Identifier: PA102406

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017552

RCV000056848

RCV001267511

ClinVar Variation:

16169

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Arg416Trp	CA217140 NM_002055.5:c.1246C>T