Canonical Allele Identifier: PA2826768088
Gene: GPI HGNC NCBI

Linked Data

ClinVar Variation Id: 13642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276719.1:p.Asp511Asn
CA123317
NM_001289790.2:c.1531G>A