Allele Registry

Canonical Allele Identifier: PA2826143569

Gene: PIGT HGNC NCBI

ClinVar RCV:

RCV000132728

RCV001531960

ClinVar Variation:

143194

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171657.1:p.Arg392Trp	CA170098 NM_001184728.3:c.1174C>T