Canonical Allele Identifier: PA2826297935
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1466016
ClinVar RCV Id: RCV001963862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Ser38Phe
CA399849069
NM_001242376.3:c.113C>T
CA645576200
NM_001242376.3:c.113_114delinsTT