Canonical Allele Identifier: PA2829353329
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1712750
ClinVar RCV Id: RCV002300922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Thr412Ser
CA399838857
NM_002055.5:c.1235C>G
CA399838864
NM_002055.5:c.1234A>T