Canonical Allele Identifier: PA2826298200
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 558829
ClinVar RCV Id: RCV000675411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Leu369Val
CA399843407
NM_001242376.3:c.1105C>G