Canonical Allele Identifier: PA2829353325
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1715460
ClinVar RCV Id: RCV002301247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Val410Leu
CA399838897
NM_002055.5:c.1228G>T
CA399838899
NM_002055.5:c.1228G>C