Canonical Allele Identifier: PA2580483012
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 2052837
ClinVar RCV Id: RCV002937748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Asn115His
CA394187234
NM_032520.5:c.343A>C