Allele Registry

Canonical Allele Identifier: PA2826143930

Gene: PIGT HGNC NCBI

ClinVar RCV:

RCV000132728

RCV001531960

ClinVar Variation:

143194

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171659.1:p.Arg346Trp	CA170098 NM_001184730.3:c.1036C>T