Canonical Allele Identifier: PA1139748489
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 856492
ClinVar RCV Id: RCV001061966 RCV001273757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Arg147Gln
CA7807704
NM_032520.5:c.440G>A