Canonical Allele Identifier: PA2580483010
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 2059325
ClinVar RCV Id: RCV002933672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.His109Tyr
CA394187185
NM_032520.5:c.325C>T