Canonical Allele Identifier: PA2826143042
Gene: GPI HGNC NCBI

Linked Data

ClinVar Variation Id: 13642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171651.1:p.Asp550Asn
CA123317
NM_001184722.1:c.1648G>A