Canonical Allele Identifier: PA2825774313
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2739845
ClinVar RCV Id: RCV003555622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124491.1:p.Thr48Ser
CA399849015
NM_001131019.3:c.143C>G
CA399849017
NM_001131019.3:c.142A>T