Canonical Allele Identifier: PA2826143683
Gene: PIGT HGNC NCBI

Linked Data

ClinVar Variation Id: 474456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171658.1:p.Arg178Gln
CA9877927
NM_001184729.3:c.533G>A