Canonical Allele Identifier: PA2826143472
Gene: PIGT HGNC NCBI

Linked Data

ClinVar Variation Id: 64649
ClinVar RCV Id: RCV000054819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171657.1:p.Thr127Pro
CA144714
NM_001184728.3:c.379A>C