Canonical Allele Identifier: PA658663043
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 472223
ClinVar RCV Id: RCV000558792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789744.1:p.Val864Ile
CA301887240
NM_176787.5:c.2590G>A