Canonical Allele Identifier: PA2827275377
Gene: GPI HGNC NCBI

Linked Data

ClinVar Variation Id: 2258621
ClinVar RCV Id: RCV002772842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316839.1:p.Arg556Ser
CA405246840
NM_001329910.1:c.1668A>C
CA405246841
NM_001329910.1:c.1668A>T