Canonical Allele Identifier: PA2828120171
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2132009
ClinVar RCV Id: RCV003062100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Met73Ile
CA399848751
NM_001363846.2:c.219G>T
CA399848753
NM_001363846.2:c.219G>C
CA399848755
NM_001363846.2:c.219G>A