Canonical Allele Identifier: PA2828120325
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 190346
ClinVar RCV Id: RCV000192145
ClinVar Variation Id: 190347
ClinVar RCV Id: RCV000192146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Leu264Pro
CA347206
NM_001363846.2:c.791T>C
CA347208
NM_001363846.2:c.791_792delinsCT