Canonical Allele Identifier: PA915995750
Gene: PIGT HGNC NCBI

Linked Data

ClinVar Variation Id: 474456
ClinVar RCV Id: RCV000539341 RCV001637081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171659.1:p.Arg76Gln
CA9877927
NM_001184730.3:c.227G>A