Canonical Allele Identifier: PA2829730394
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 1696901
ClinVar RCV Id: RCV002267247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036459.1:p.Ser194Phe
CA402602261
NM_012327.6:c.581C>T