Canonical Allele Identifier: PA2826143037
Gene: GPI HGNC NCBI

Linked Data

ClinVar Variation Id: 1031448
ClinVar RCV Id: RCV001333274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171651.1:p.Ser543Thr
CA9367489
NM_001184722.1:c.1628G>C