Canonical Allele Identifier: PA1139748441
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 938074
ClinVar RCV Id: RCV001207224 RCV001833822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Asn115Thr
CA394187237
NM_032520.5:c.344A>C