Canonical Allele Identifier: PA2826298092
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66496
ClinVar RCV Id: RCV000056897 RCV000192134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Lys236Thr
CA217207
NM_001242376.3:c.707A>C