Canonical Allele Identifier: PA217110
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66433
ClinVar RCV Id: RCV000056827 RCV000192166
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Ala364Val
CA217109
NM_002055.5:c.1091C>T