Canonical Allele Identifier: PA102560
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 16179
ClinVar RCV Id: RCV000017562 RCV003556033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Asp78Glu
CA341388
NM_002055.5:c.234C>A
CA399848688
NM_002055.5:c.234C>G