Canonical Allele Identifier: PA2829189521
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_001378849.1:p.Pro487Leu
CA232364
NM_001391920.1:c.1460C>T