Canonical Allele Identifier: PA2828120297
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2840017
ClinVar RCV Id: RCV003716150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Ala234Thr
CA399845758
NM_001363846.2:c.700G>A