Canonical Allele Identifier: PA102856
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 190334
ClinVar RCV Id: RCV000192103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Met73Thr
CA347186
NM_002055.5:c.218T>C