Canonical Allele Identifier: PA2580532763
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 2095041
ClinVar RCV Id: RCV003012141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789744.1:p.Asp869Gly
CA402723571
NM_176787.5:c.2606A>G