Canonical Allele Identifier: PA2829730893
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 1007807
ClinVar RCV Id: RCV001305046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036459.1:p.Ser891Gly
CA402723416
NM_012327.6:c.2671A>G