Allele Registry

Canonical Allele Identifier: PA102614

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000017559

RCV000056825

ClinVar Variation:

16176

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Glu362Asp	CA217107 NM_002055.5:c.1086G>C CA399843488 NM_002055.5:c.1086G>T