Canonical Allele Identifier: PA2826298169
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 265178
ClinVar RCV Id: RCV000254720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Gly335Arg
CA8608773
NM_001242376.3:c.1003G>A
CA399844083
NM_001242376.3:c.1003G>C