Canonical Allele Identifier: PA2829730533
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 1905584
ClinVar RCV Id: RCV002583616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036459.1:p.Phe399Cys
CA402606187
NM_012327.6:c.1196T>G