Canonical Allele Identifier: PA2829730404
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 1753881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036459.1:p.Gly217Arg
CA402602026
NM_012327.6:c.649G>C
CA402602028
NM_012327.6:c.649G>A