Allele Registry

Canonical Allele Identifier: PA170099

Gene: PIGT HGNC NCBI

ClinVar RCV:

RCV000132728

RCV001531960

ClinVar Variation:

143194

HGVS (amino-acid)	Matching Registered Transcripts
NP_057021.2:p.Arg448Trp	CA170098 NM_015937.6:c.1342C>T