Canonical Allele Identifier: PA102350
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66497
ClinVar RCV Id: RCV000056900 RCV000192136
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Arg239Pro
CA217210
NM_002055.5:c.716G>C