Canonical Allele Identifier: PA658663262
Gene: PIGT HGNC NCBI

Linked Data

ClinVar Variation Id: 474456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057021.2:p.Arg178Gln
CA9877927
NM_015937.6:c.533G>A