Canonical Allele Identifier: PA1139748416
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 942344
ClinVar RCV Id: RCV001212319 RCV001833860 RCV004033852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Asn99Asp
CA7807590
NM_032520.5:c.295A>G