Canonical Allele Identifier: PA1139704316
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 994616
ClinVar RCV Id: RCV001288189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Arg11Cys
CA8609129
NM_002055.5:c.31C>T