Canonical Allele Identifier: PA2825781360
Gene: GBP5 HGNC NCBI

Linked Data

ClinVar Variation Id: 92020
ClinVar RCV Id: RCV000122577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127958.1:p.Pro582Leu
CA232364
NM_001134486.4:c.1745C>T