Canonical Allele Identifier: PA2829730501
Gene: PIGN HGNC NCBI

Linked Data

ClinVar Variation Id: 402190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036459.1:p.Ile332Met
CA16609540
NM_012327.6:c.996T>G