Canonical Allele Identifier: PA2826297966
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2759752
ClinVar RCV Id: RCV003571827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Met74Ile
CA399848736
NM_001242376.3:c.222G>T
CA399848738
NM_001242376.3:c.222G>C
CA399848739
NM_001242376.3:c.222G>A