Canonical Allele Identifier: PA2829730414
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 2156467
ClinVar RCV Id: RCV003075479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036459.1:p.Ser224Ala
CA402601941
NM_012327.6:c.670T>G