Canonical Allele Identifier: PA2827275372
Gene: GPI HGNC NCBI

Linked Data

ClinVar Variation Id: 13642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316839.1:p.Asp539Asn
CA123317
NM_001329910.1:c.1615G>A