Canonical Allele Identifier: PA645431123
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 402190
ClinVar RCV Id: RCV000454324 RCV000578405 RCV003314594 RCV003401442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789744.1:p.Ile332Met
CA16609540
NM_176787.5:c.996T>G