Canonical Allele Identifier: PA217192
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66484
ClinVar RCV Id: RCV000056885 RCV000192126
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Asp128Asn
CA217191
NM_002055.5:c.382G>A