Canonical Allele Identifier: PA2741889080
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2739845
ClinVar RCV Id: RCV003555622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Thr48Ser
CA399849015
NM_002055.5:c.143C>G
CA399849017
NM_002055.5:c.142A>T