Canonical Allele Identifier: PA2826297920
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2870392
ClinVar RCV Id: RCV003703239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Met21Ile
CA399849157
NM_001242376.3:c.63G>T
CA399849158
NM_001242376.3:c.63G>A
CA399849159
NM_001242376.3:c.63G>C