Canonical Allele Identifier: PA102387
Gene: GFAP HGNC NCBI
ClinVar RCV:
RCV000056917
ClinVar Variation:
66513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Arg330Gly
CA217233
NM_002055.5:c.988C>G