Canonical Allele Identifier: PA2829730389
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 422474
ClinVar RCV Id: RCV000481779 RCV001204694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036459.1:p.His188Tyr
CA8982544
NM_012327.6:c.562C>T