Canonical Allele Identifier: PA2829730875
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 472223
ClinVar RCV Id: RCV000558792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036459.1:p.Val864Ile
CA301887240
NM_012327.6:c.2590G>A