Canonical Allele Identifier: PA2741889082
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2851474
ClinVar RCV Id: RCV003691167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Ser53Ala
CA8609086
NM_002055.5:c.157T>G