Canonical Allele Identifier: PA2826143468
Gene: PIGT HGNC NCBI

Linked Data

ClinVar Variation Id: 474456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171657.1:p.Arg122Gln
CA9877927
NM_001184728.3:c.365G>A