Canonical Allele Identifier: PA658805288
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 539554
ClinVar RCV Id: RCV000649307 RCV001569047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789744.1:p.His218Gln
CA301686018
NM_176787.5:c.654T>G
CA402602005
NM_176787.5:c.654T>A