Canonical Allele Identifier: PA1139747220
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 956208
ClinVar RCV Id: RCV001228968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789744.1:p.Arg221Gln
CA301685979
NM_176787.5:c.662G>A