Allele Registry

Canonical Allele Identifier: PA102866

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056861

RCV000192102

ClinVar Variation:

66466

HGVS (amino-acid)	Matching Registered Transcripts
NP_002046.1:p.Met74Thr	CA217158 NM_002055.5:c.221T>C