Canonical Allele Identifier: PA2828120189
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66472
ClinVar RCV Id: RCV000056871 RCV000192112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Arg79Leu
CA217169
NM_001363846.2:c.236G>T