Canonical Allele Identifier: PA2499301277
Gene: PIGN HGNC NCBI
ClinVar RCV:
RCV001305046
ClinVar Variation:
1007807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789744.1:p.Ser891Gly
CA402723416
NM_176787.5:c.2671A>G