Canonical Allele Identifier: PA2828120408
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1077122
ClinVar RCV Id: RCV001391254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Leu370Pro
CA399843384
NM_001363846.2:c.1109T>C